Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer
BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To me...
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description | BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction. |
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Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.</description><identifier>ISSN: 1076-0512</identifier><identifier>EISSN: 1524-4725</identifier><identifier>DOI: 10.1097/DSS.0000000000002473</identifier><identifier>PMID: 33565773</identifier><language>eng</language><publisher>PHILADELPHIA: Lippincott Williams & Wilkins</publisher><subject>Aged ; Biopsy - statistics & numerical data ; Carcinoma, Basal Cell - diagnosis ; Carcinoma, Basal Cell - pathology ; Carcinoma, Basal Cell - surgery ; Carcinoma, Squamous Cell - diagnosis ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - surgery ; Dermatology ; Female ; Frozen Sections - statistics & numerical data ; Humans ; Keratosis, Actinic - diagnosis ; Keratosis, Actinic - pathology ; Keratosis, Actinic - surgery ; Life Sciences & Biomedicine ; Male ; Mohs Surgery - statistics & numerical data ; Observer Variation ; Reproducibility of Results ; Retrospective Studies ; Science & Technology ; Skin - pathology ; Skin Neoplasms - diagnosis ; Skin Neoplasms - pathology ; Skin Neoplasms - surgery ; Surgery</subject><ispartof>Dermatologic surgery, 2021-02, Vol.47 (2), p.194-199</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2020 by the American Society for Dermatologic Surgery, Inc. Published by Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>3</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000635109500016</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c3528-fe0cdccf644ea43c4bd3dc90abb1962b265e9770e909e14d2d485686e14c4e813</citedby><cites>FETCH-LOGICAL-c3528-fe0cdccf644ea43c4bd3dc90abb1962b265e9770e909e14d2d485686e14c4e813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934,39267</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33565773$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mulvaney, Patrick M.</creatorcontrib><creatorcontrib>Piris, Adriano</creatorcontrib><creatorcontrib>Besaw, Robert J.</creatorcontrib><creatorcontrib>Schmults, Chrysalyne D.</creatorcontrib><title>Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer</title><title>Dermatologic surgery</title><addtitle>DERMATOL SURG</addtitle><addtitle>Dermatol Surg</addtitle><description>BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.</description><subject>Aged</subject><subject>Biopsy - statistics & numerical data</subject><subject>Carcinoma, Basal Cell - diagnosis</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Carcinoma, Basal Cell - surgery</subject><subject>Carcinoma, Squamous Cell - diagnosis</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - surgery</subject><subject>Dermatology</subject><subject>Female</subject><subject>Frozen Sections - statistics & numerical data</subject><subject>Humans</subject><subject>Keratosis, Actinic - diagnosis</subject><subject>Keratosis, Actinic - pathology</subject><subject>Keratosis, Actinic - surgery</subject><subject>Life Sciences & Biomedicine</subject><subject>Male</subject><subject>Mohs Surgery - statistics & numerical data</subject><subject>Observer Variation</subject><subject>Reproducibility of Results</subject><subject>Retrospective Studies</subject><subject>Science & Technology</subject><subject>Skin - pathology</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - surgery</subject><subject>Surgery</subject><issn>1076-0512</issn><issn>1524-4725</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>EIF</sourceid><recordid>eNqNkE1PFTEUhhuDEUT_gSFdkpDBfne6xEGUhMji4nrS6ZyRwkx7aWe4wV9vby6icWU3PU2e95yeB6EPlJxSYvTH89XqlPx1mND8FTqgkolKaCb3Sk20qoikbB-9zfmOEMoMJ2_QPudSSa35Abo59_ZHiHn2Dn_ycZ2f8KO3-DJU18PgHeCLFH9CwCtws48h4yEm3Iw-eGdH_C2GCUYb4mTx6t4H3NjgIL1Drwc7Znj_fB-i7xefb5qv1dX1l8vm7KpyXLK6GoC43rlBCQFWcCe6nvfOENt11CjWMSXBaE3AEANU9KwXtVS1KrUTUFN-iI53fdcpPiyQ53by2cFYfgRxyS0TdU2N0YQXVOxQl2LOCYZ2nfxk01NLSbv12Raf7b8-S-zoecLSTdC_hH4LLMDJDthAF4fsPBQBL1hpo7gs7WWpqCp0_f9042e7dd7EJcx_FtjEcYaU78dlA6m9BTvOt9uoYLo4ZYRRwsqz2u5Q818ehZ__</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Mulvaney, Patrick M.</creator><creator>Piris, Adriano</creator><creator>Besaw, Robert J.</creator><creator>Schmults, Chrysalyne D.</creator><general>Lippincott Williams & Wilkins</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210201</creationdate><title>Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer</title><author>Mulvaney, Patrick M. ; Piris, Adriano ; Besaw, Robert J. ; Schmults, Chrysalyne D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3528-fe0cdccf644ea43c4bd3dc90abb1962b265e9770e909e14d2d485686e14c4e813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Biopsy - statistics & numerical data</topic><topic>Carcinoma, Basal Cell - diagnosis</topic><topic>Carcinoma, Basal Cell - pathology</topic><topic>Carcinoma, Basal Cell - surgery</topic><topic>Carcinoma, Squamous Cell - diagnosis</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - surgery</topic><topic>Dermatology</topic><topic>Female</topic><topic>Frozen Sections - statistics & numerical data</topic><topic>Humans</topic><topic>Keratosis, Actinic - diagnosis</topic><topic>Keratosis, Actinic - pathology</topic><topic>Keratosis, Actinic - surgery</topic><topic>Life Sciences & Biomedicine</topic><topic>Male</topic><topic>Mohs Surgery - statistics & numerical data</topic><topic>Observer Variation</topic><topic>Reproducibility of Results</topic><topic>Retrospective Studies</topic><topic>Science & Technology</topic><topic>Skin - pathology</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - surgery</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mulvaney, Patrick M.</creatorcontrib><creatorcontrib>Piris, Adriano</creatorcontrib><creatorcontrib>Besaw, Robert J.</creatorcontrib><creatorcontrib>Schmults, Chrysalyne D.</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Dermatologic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mulvaney, Patrick M.</au><au>Piris, Adriano</au><au>Besaw, Robert J.</au><au>Schmults, Chrysalyne D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer</atitle><jtitle>Dermatologic surgery</jtitle><stitle>DERMATOL SURG</stitle><addtitle>Dermatol Surg</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>47</volume><issue>2</issue><spage>194</spage><epage>199</epage><pages>194-199</pages><issn>1076-0512</issn><eissn>1524-4725</eissn><abstract>BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.</abstract><cop>PHILADELPHIA</cop><pub>Lippincott Williams & Wilkins</pub><pmid>33565773</pmid><doi>10.1097/DSS.0000000000002473</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Biopsy - statistics & numerical data Carcinoma, Basal Cell - diagnosis Carcinoma, Basal Cell - pathology Carcinoma, Basal Cell - surgery Carcinoma, Squamous Cell - diagnosis Carcinoma, Squamous Cell - pathology Carcinoma, Squamous Cell - surgery Dermatology Female Frozen Sections - statistics & numerical data Humans Keratosis, Actinic - diagnosis Keratosis, Actinic - pathology Keratosis, Actinic - surgery Life Sciences & Biomedicine Male Mohs Surgery - statistics & numerical data Observer Variation Reproducibility of Results Retrospective Studies Science & Technology Skin - pathology Skin Neoplasms - diagnosis Skin Neoplasms - pathology Skin Neoplasms - surgery Surgery |
title | Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer |
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